Zobrazeno 1 - 10
of 561
pro vyhledávání: '"Masaki Watanabe"'
Autor:
Kosei Nakamura, Yasuko Kuroha, Masahiro Hatakeyama, Atsushi Michael Kimura, Yukimi Nakamura, Yoshihiro Murakami, Masaki Watanabe, Hironaka Igarashi, Tetsuya Takahashi, Hitoshi Shimada
Publikováno v:
BMC Geriatrics, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background Corticobasal syndrome (CBS) is a neurodegenerative disease diagnosed based on clinical manifestations such as asymmetrical parkinsonism, limb apraxia, and speech and language impairment. The background pathology of CBS is commonly
Externí odkaz:
https://doaj.org/article/a8af366b868c480a95654de25107f9f6
Publikováno v:
Genes, Vol 15, Iss 4, p 456 (2024)
The Adriamycin (ADR) nephropathy model, which induces podocyte injury, is limited to certain mouse strains due to genetic susceptibilities, such as the PrkdcR2140C polymorphism. The FVB/N strain without the R2140C mutation resists ADR nephropathy. Me
Externí odkaz:
https://doaj.org/article/51a5e82ccaec4a3598902505f8874f7e
Autor:
Koki Hiura, Masaki Watanabe, Naoki Hirose, Kenta Nakano, Tadashi Okamura, Hayato Sasaki, Nobuya Sasaki
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 5, p 3061 (2024)
Patients with inflammatory bowel disease (IBD) who experience long-term chronic inflammation of the colon are at an increased risk of developing colorectal cancer (CRC). Mitotic spindle positioning (MISP), an actin-binding protein, plays a role in mi
Externí odkaz:
https://doaj.org/article/f89d66c7195845699c7e0a2cc4f8b11f
Autor:
Chihiro Yagi, Yuka Morita, Tatsuya Yamagishi, Shinsuke Ohshima, Shuji Izumi, Kuniyuki Takahashi, Masaki Watanabe, Kosuke Itoh, Yuji Suzuki, Hironaka Igarashi, Arata Horii
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
IntroductionPersistent postural-perceptual dizziness (PPPD) is a functional chronic vestibular syndrome with symptom exacerbation by upright posture, motion, and complex visual stimuli. Among these exacerbating factors, visual exacerbation is the mos
Externí odkaz:
https://doaj.org/article/02ed991a289543199f8133da6c60dc9e
Publikováno v:
IJU Case Reports, Vol 5, Iss 5, Pp 389-392 (2022)
Introduction This report aims to describe our experience in the pelvic floor reconstruction of anterior enterocele following radical cystectomy by transvaginal surgery using a mesh for abdominal wall hernia repair. Case presentation An 84‐years‐o
Externí odkaz:
https://doaj.org/article/adf4e826fc4a4b5eb1b67d329bee844f
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract Individuals with Prader–Willi syndrome (PWS) exhibit complex behavioral characteristics, including hyperphagia, autistic features, and subsequent age-related maladaptive behaviors. While this suggests functional involvements of subcortical
Externí odkaz:
https://doaj.org/article/3e87c116824a4fce9749205617ae9df1
Autor:
Tomomi Miyoshi, Masaki Watanabe
Publikováno v:
PLoS ONE, Vol 18, Iss 3, p e0283432 (2023)
In promoting genomic medicine, genomic literacy, which is the public's ability to acquire and utilize the knowledge and skills related to genetics and genomes, requires urgent improvement. This study determined how the three components of genomic lit
Externí odkaz:
https://doaj.org/article/cb155a803a294e46a113cdc0cbcedb89
Autor:
Masaki Watanabe, Koya Shishido, Nao Kanehira, Koki Hiura, Kenta Nakano, Tadashi Okamura, Ryo Ando, Hayato Sasaki, Nobuya Sasaki
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 8, p 6955 (2023)
Most mitochondrial diseases are hereditary and highly heterogeneous. Cattle born with the V79L mutation in the isoleucyl-tRNA synthetase 1 (IARS1) protein exhibit weak calf syndrome. Recent human genomic studies about pediatric mitochondrial diseases
Externí odkaz:
https://doaj.org/article/d79509fb01284433a03223e98995ca32
Autor:
Saori Sakaue, Etsuro Yamaguchi, Yoshikazu Inoue, Meiko Takahashi, Jun Hirata, Ken Suzuki, Satoru Ito, Toru Arai, Masaki Hirose, Yoshinori Tanino, Takefumi Nikaido, Toshio Ichiwata, Shinya Ohkouchi, Taizou Hirano, Toshinori Takada, Satoru Miyawaki, Shogo Dofuku, Yuichi Maeda, Takuro Nii, Toshihiro Kishikawa, Kotaro Ogawa, Tatsuo Masuda, Kenichi Yamamoto, Kyuto Sonehara, Ryushi Tazawa, Konosuke Morimoto, Masahiro Takaki, Satoshi Konno, Masaru Suzuki, Keisuke Tomii, Atsushi Nakagawa, Tomohiro Handa, Kiminobu Tanizawa, Haruyuki Ishii, Manabu Ishida, Toshiyuki Kato, Naoya Takeda, Koshi Yokomura, Takashi Matsui, Masaki Watanabe, Hiromasa Inoue, Kazuyoshi Imaizumi, Yasuhiro Goto, Hiroshi Kida, Tomoyuki Fujisawa, Takafumi Suda, Takashi Yamada, Yasuomi Satake, Hidenori Ibata, Nobuyuki Hizawa, Hideki Mochizuki, Atsushi Kumanogoh, Fumihiko Matsuda, Koh Nakata, Tomomitsu Hirota, Mayumi Tamari, Yukinori Okada
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-6 (2021)
Autoimmune pulmonary alveolar proteinosis (aPAP) is a complex lung disease caused by abnormal surfactant homeostasis. Here, the authors carry out a genome-wide association study of aPAP in a Japanese cohort, finding variants in the MHC and suggesting
Externí odkaz:
https://doaj.org/article/d9a62f084a8e4179916af621aeb86739
Publikováno v:
Biomarkers in Neuropsychiatry, Vol 5, Iss , Pp 100039- (2021)
Prader-Willi syndrome is a complex endocrinological and developmental disorder characterized by hyperphagic, autistic, and obsessive behaviors, which have been considered to primarily originate from hypothalamus-pituitary axis system alterations in t
Externí odkaz:
https://doaj.org/article/dd11d61b58b94cf6b3b14dfaf5d71679